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一例伴有硬皮病的食管增生性息肉罕见病例:病例报告及文献复习

An Unusual Case of Esophageal Hyperplastic Polyp with Scleroderma: A Case Report and Review of the Literature.

作者信息

Tarar Zahid Ijaz, Tahan Veysel, Yin Feng, Daglilar Ebubekir

机构信息

Internal Medicine, University of Missouri-Columbia, Columbia, USA.

Gastroenterology & Hepatology, University of Missouri-Columbia, Columbia, USA.

出版信息

Cureus. 2021 Jan 5;13(1):e12500. doi: 10.7759/cureus.12500.

DOI:10.7759/cureus.12500
PMID:33564508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7861061/
Abstract

Hyperplastic polyp of the esophagus is a rare condition and most of the time asymptomatic. We report a case of a 69-year-old female with scleroderma who presented with worsening dysphagia, regurgitation of food, and non-cardiac chest pain. Upper endoscopy showed a nodular lesion in the distal esophagus. Biopsy of the lesion showed features of hyperplastic polyp without any metaplastic changes. She was started on anti-acid therapy and an outpatient upper endoscopy was performed which showed no residual polyp.

摘要

食管增生性息肉是一种罕见病症,多数情况下无症状。我们报告一例69岁患硬皮病的女性患者,其出现吞咽困难加重、食物反流和非心源性胸痛症状。上消化道内镜检查显示食管远端有一个结节性病变。该病变活检显示为增生性息肉特征,无任何化生改变。给予她抗酸治疗,并进行了门诊上消化道内镜检查,结果显示无残留息肉。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0142/7861061/837c8d5a298c/cureus-0013-00000012500-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0142/7861061/51658952a18e/cureus-0013-00000012500-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0142/7861061/bcace761792c/cureus-0013-00000012500-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0142/7861061/837c8d5a298c/cureus-0013-00000012500-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0142/7861061/51658952a18e/cureus-0013-00000012500-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0142/7861061/bcace761792c/cureus-0013-00000012500-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0142/7861061/837c8d5a298c/cureus-0013-00000012500-i03.jpg

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本文引用的文献

1
Upper gastrointestinal tract polyps: what do we know about them?上消化道息肉:我们对它们了解多少?
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Benign esophageal lesions: endoscopic and pathologic features.良性食管病变:内镜及病理特征
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J Med Case Rep. 2007 Nov 2;1:127. doi: 10.1186/1752-1947-1-127.
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